FDA 510(k) FDA class 2 Substantially Equivalent 🇮🇱 Israel

GENASIS SCANVIEW SYSTEM

K Number: K122554 · Decision Feb 7, 2013
Classifications
1
FEI Numbers
3
Registration Numbers
3
Same Product Code
7
Applicant Total
7
Review Days
170

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Basic Information

Device Name
GENASIS SCANVIEW SYSTEM
K Number
K122554
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.4700
Medical Specialty
Immunology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Applied Spectral Imaging , Ltd.
Date Received
August 21, 2012
Decision Date
February 7, 2013
Product Code
NTH
Advisory Committee
Immunology
Review Advisory Committee
PA
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
NTH System, Automated Scanning Microscope And Image Analysis For Fluorescence In Situ Hybridization (Fish) Assays

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (NTH), ordered by most recent decision date.

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Other Clearances by Applied Spectral Imaging , Ltd.

K Number Device Name
K140957 GENASIS HIPATH IHC FAMILY
K101291 SCANVIEW HER2/NEU FISH SYSTEM
K071398 SCANVIEW, MODEL SC-300
K050236 FISHVIEW
K012103 BANDVIEW SYSTEM
K973950 RETINAL CUBE